Vy Spine, LLC

Vy Spine, LLC — FDA 510(k) Submissions

Vy Spine, LLC has submitted 19 FDA 510(k) premarket notifications since 2021, of which 19 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Intervertebral Fusion Device With Bone Graft, Cervical, Intervertebral Fusion Device With Bone Graft, Lumbar, Posterior Cervical Screw System, Appliance, Fixation, Spinal Intervertebral Body, Thoracolumbosacral Pedicle Screw System . Use the specialty filter in the sidebar to narrow results.